Clinical Research Coordinators
Also called: Clinical Research Coordinator, Clinical Trial Manager, Clinical Program Manager, Clinical Research Associate (CRA)
What they do:
Plan, direct, or coordinate clinical research projects. Direct the activities of workers engaged in clinical research projects to ensure compliance with protocols and overall clinical objectives. May evaluate and analyze clinical data.
On the job, you would:
- Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms.
- Oversee subject enrollment to ensure that informed consent is properly obtained and documented.
- Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.
Arts and Humanities
Health
Business
Math and Science
|
Basic Skills
Problem Solving
Social
|
Verbal
Ideas and Logic
Attention
|
People interested in this work like activities that include
leading, making decisions, and business. They do well at jobs that need:
|
You might use software like this on the job: Data base user interface and query software
Analytical or scientific software
Electronic mail software
|
|
|
You might like a career in one of these industries:
|
See more details at O*NET OnLine about clinical research coordinators.